IN VIVO Attachable and Detachable End Effector Assembly and Laparoscopic Surgical Instrument and Methods Therefor

ABSTRACT

A method of performing surgery includes the steps of providing a forceps having a housing including a shaft that extends therefrom and at least one handle moveable relative to the housing and providing an end effector assembly configured to selectively engage a distal end of the shaft. The method also includes the steps of inserting the forceps through a first opening formed in a body; inserting the end effector assembly through a second opening formed in the body; engaging the end effector assembly with the distal end of the shaft in vivo; and actuating the end effector assembly by moving the handle relative to the housing. The method may also include the steps of providing a coupling at the distal end of the shaft, and engaging, via the coupling, the distal end of the shaft with the end effector assembly.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No.12/562,281 by Dumbauld et al., “IN VIVO ATTACHABLE AND DETACHABLE ENDEFFECTOR ASSEMBLY AND LAPAROSCOPIC SURGICAL INSTRUMENT AND METHODSTHEREFOR”, filed on Sep. 18, 2009, and published as U.S. PatentApplication Publication US 2011/0071522 A1 “IN VIVO ATTACHABLE ANDDETACHABLE END EFFECTOR ASSEMBLY AND LAPAROSCOPIC SURGICAL INSTRUMENTAND METHODS THEREFOR”, the entire contents of each of which isincorporated by reference herein.

BACKGROUND

1. Technical Field

The present disclosure relates to endoscopic or laparoscopic surgery andmore particularly to end effector assemblies for surgical instrumentsused therein.

2. Description of the Related Art

The trend in surgical procedures is to reduce the invasiveness of theprocedure by reducing the size of the surgical incision. More and morefrequently, the surgical incision is performed in the navel of thepatient. For a laparoscopic surgical instrument, the outer shaftdiameter is determined by the inner diameter of the ports (cannulae)with which the instrument will be used. As port size decreases toaccommodate the reduced size of the surgical incision, thediameter/cross-sectional area of the end effectors of the surgicalinstrument must be reduced while the length of the end effectors mustalso be reduced to provide greater rigidity to reduce the susceptibilityof the end effectors to deflection.

The resulting rigidity of the end effectors of the instrument therebynecessitates tight dimensional tolerances and a corresponding increasein material and manufacturing costs to provide the necessary rigidity.

SUMMARY

To advance the state of the art of surgery, the present disclosurerelates to a method of performing surgery that includes the steps ofproviding a forceps having a housing including a shaft that extendstherefrom and at least one handle moveable relative to the housing andproviding an end effector assembly configured to selectively engage adistal end of the shaft. The method also includes the steps of insertingthe forceps through a first opening formed in a body; inserting the endeffector assembly through a second opening formed in the body; engagingthe end effector assembly with the distal end of the shaft in vivo; andactuating the end effector assembly by moving the handle relative to thehousing.

The method may include the step of providing a coupling at the distalend of the shaft, and may further include the step of engaging, via thecoupling, the distal end of the shaft with the end effector assembly.

BRIEF DESCRIPTION OF THE DRAWINGS

Various embodiments of the present disclosure are described herein withreference to the drawings wherein:

FIG. 1A illustrates a beam having a rectangular cross-section and thecorresponding equation and dimensions to calculate the moment of inertiaof the beam around a particular axis;

FIG. 1B illustrates a cantilevered beam and the correspondingmathematical factors related to calculating the deflection of the beamalong the length of the beam with respect to the anchor point;

FIG. 1C illustrates the cantilevered beam of FIG. 1B and the equationsto calculate the deflection of the beam under a load as a function ofthe distance along the length of the beam with respect to the anchorpoint;

FIG. 1D illustrates the cantilevered beam of FIG. 1B and the equationsto calculate the deflection of the beam under a bending moment as afunction of the distance along the length of the beam with respect tothe anchor point;

FIG. 2 is a left, perspective view of an endoscopic bipolar forcepsshowing a housing, a shaft and an in vivo detachable end effectorassembly according to one embodiment of the present disclosure;

FIG. 3A is an enlarged, left, perspective view of the end effectorassembly and shaft of FIG. 1 in which the in vivo detachable endeffector assembly is in an open position;

FIG. 3B is a an enlarged, left, perspective view of the end effectorassembly and shaft of FIG. 1 in which the in vivo detachable endeffector assembly is in a closed position;

FIG. 4 is a left, perspective, exploded view of the shaft and push rodof the in vivo detachable end effector assembly;

FIG. 5 is a detailed, left, perspective, exploded view of the jawmembers of the in vivo detachable end effector assembly;

FIG. 6 is a right, perspective view of the in vivo detachable endeffector assembly and the shaft generally joined by a coupling accordingto one embodiment of the present disclosure;

FIG. 7 is a right, perspective view of the in vivo detachable endeffector assembly and the shaft joined by a compression couplingaccording to one embodiment of the present disclosure;

FIG. 8 is a simplified view of an abdominal cavity in a subjectillustrating an in vivo method of attaching a detachable end effectorassembly to an endoscopic surgical instrument during a laparoscopicprocedure according to one embodiment of the present disclosure;

FIG. 9 is a simplified view of an abdominal cavity in a subjectillustrating an in vivo method of attaching, via a grasping device, adetachable end effector assembly to an endoscopic surgical instrumentduring a laparoscopic procedure according to another embodiment of thepresent disclosure; and

FIG. 10 is a simplified view of an abdominal cavity in a subjectillustrating an in vivo method of attaching a detachable end effectorassembly to an endoscopic surgical instrument during a laparoscopicprocedure via a coupling that is configured to interface with the endeffector assembly and the endoscopic surgical instrument according tostill another embodiment of the present disclosure.

DETAILED DESCRIPTION

Various embodiments of the present disclosure are described hereinbelowwith reference to the accompanying drawings. Well-known functions orconstructions are not described in detail to avoid obscuring the presentdisclosure in unnecessary detail.

The present disclosure relates to a laparoscopic surgical instrumenthaving a mating joint to enable attachment and detachment of adetachable end effector. The detachable end effector may be introducedinto the abdominal cavity through a surgical incision such as at thenavel while the laparoscopic surgical instrument is introduced, withoutthe detachable end effector, into the abdominal cavity through anothersurgical incision. Alternatively, the detachable end effector may beintroduced through a natural orifice such as the anal canal, while thelaparoscopic surgical instrument is introduced, without the detachableend effector, through a surgical incision in the abdominal cavity.

The detachable end effector may be introduced by a second instrument,such as a grasper, which is used to attach or connect the detachable endeffector to the mating joint of the instrument.

As compared to conventional laparoscopic surgical instruments, since thedetachable end effector is introduced through a natural orifice of thepatient, the length and the diameter of the detachable end effector ofthe laparoscopic surgical instrument according to the embodiments of thepresent disclosure may be increased.

Removal of the diameter and length constraints of the end effectors ofthe prior art generally allows for looser tolerances and more costeffective end effector fabrication processes. As the diameter is asignificant factor in determining the necessary rigidity of the endeffector assembly, a larger-diameter end effector assembly can be alonger end effector assembly because the end effector assembly will beless susceptible to deflection and thus provide a more uniformdistribution of sealing pressure to the tissue.

As is well-known in the art, deflection of a cantilevered beam, whichcan approximate the deflection of the end effector assembly with respectto the shaft of the endoscopic instrument, is directly proportional tothe distance of the applied load from an anchor point, in this case, thejoint between the end effector assembly and the shaft, and inverselyproportional to Young's modulus of elasticity E and the moment ofinertia I of the end effector assembly, as illustrated in FIGS. 1A-1D.For an assumed rectangular cross-section 2′ of the beam 2 as illustratedin FIG. 1A, since the moment of inertia I_(x) around the x-axis isproportional to the width b times the cube of the height h, i.e., h³, itcan be seen that an increase in height h, while b remains constant,significantly increases the moment of inertia I_(x). As can then be seenfrom FIGS. 1B-1C, if the beam 2 is assumed to be a cantilevered beamanchored at anchor point 4, representing the distal end of a shaft of anendoscopic instrument, the deflection v in the y-direction is directlyproportional to the applied load P and the cube of the distance a fromthe anchor point 4, i.e., a³. Since the load P and the cube of thedistance a are independent of the moment of inertia I_(X), it can thenbe understood that any increase in moment of inertia I_(x) (while theother factors remain the same) will reduce the deflection v. FIG. 1Dsimply illustrates the same effect if one assumes a bending moment M₀around anchor point 4 instead of load P.

Following completion of the surgical procedure, the detachable endeffector having an enlarged moment of inertia and rigidity is detachedfrom the mating joint via the second instrument, which may again beintroduced through the natural orifice and used to withdraw thedetachable end effector from the abdominal cavity while the laparoscopicsurgical instrument is withdrawn through the surgical incision.

In the drawings and in the descriptions which follow, the term“proximal”, as is traditional, will refer to the end of the forceps 10which is closer to the user, while the term “distal” will refer to theend which is further from the user. It should be noted that with respectto the end effector assembly 100, reference to proximal end and distalend will be with respect to configuration of the end effector assembly100 following attachment to the distal end 14 of the shaft 12 andcorresponding actual use via the endoscopic bipolar forceps 10 duringthe surgical procedure, as opposed to the position of the end effectorassembly 100 during the attachment process.

Referring now to FIG. 2, a tissue sealing system 3 having a combinationforceps and in vivo detachable end effector assembly 5 according to thepresent disclosure is shown. The combination forceps and in vivodetachable end effector assembly 5 includes a forceps 10 coupled to agenerator 20. Upon attachment and engagement of end effector assembly100, as described in more detail below, the combination forceps and invivo detachable end effector assembly 5 is adapted to seal tissue usingelectrosurgical energy. The generator 20 may be configured to outputvarious types of electrosurgical energy (e.g., from about 300 MHz toabout 10,000 MHz).

The forceps 10 is coupled to the generator 20 via a cable 11 adapted totransmit energy and control signals therebetween. Various embodiments ofthe forceps 10 utilizing the aforementioned types of energy arediscussed in more detail below.

As indicated, the forceps 10 is configured to support an in vivodetachable end effector assembly 100. Forceps 10 typically includesvarious conventional features (e.g., a housing 60, a handle assembly 75,a rotating assembly 80, a trigger assembly 70) which enable forceps 10and detachable end effector assembly 100 to mutually cooperate to grasp,seal and, if warranted, divide tissue. Forceps 10 generally includeshousing 60 and handle assembly 75, which includes moveable handle 62 andhandle 72 that is integral with housing 60. Handle 62 is moveablerelative to handle 72 to actuate detachable end effector assembly 100 tograsp and treat tissue. Forceps 10 also includes a shaft 12 that hasdistal end 14 that mechanically engages detachable end effector assembly100 and proximal end 16 that mechanically engages housing 60 proximaterotating assembly 80 disposed at the distal end of housing 60. Rotatingassembly 80 is mechanically associated with shaft 12. Movement ofrotating assembly 80 imparts similar rotational movement to shaft 12which, in turn, rotates detachable end effector assembly 100.

Referring also to FIGS. 3A-3B, detachable end effector assembly 100includes a proximal end 1250 comprising a shaft 1201 at proximal end1250 that is configured to engage distal end 14 of the shaft 12 of theforceps 10 at interface joint 140. The engagement between the shaft 12and the shaft 1201 at interface joint 140 enables the attachment anddetachment of the end effector assembly 100 with the forceps 10.

Detachable end effector assembly 100 also includes two jaw members 110and 120 having proximal ends 111, 121 and distal ends 114, 124. Jawmembers 110 and 120 are pivotable about a post or pivot pin 95 and aremovable from a first position wherein jaw members 110 and 120 are spacedrelative to another, to a second position wherein jaw members 110 and120 are closed and cooperate to grasp tissue therebetween. As discussedin more detail below, the detachable end effector assembly 100 may beadapted for use with various energy sources.

In the illustrated embodiment, the shaft 12 houses a pushrod 101 that isoperatively coupled to the movable handle 62 such that when the handle62 is moved relative to the handle 72 the pushrod 101 moveslongitudinally, either proximally or distally within the shaft 12. Thepushrod 101 may include one or more pins disposed at the distal end 16of shaft 12. Each of the jaw members 110 and 120 includes acorresponding slot disposed at the proximal ends thereof thatmechanically cooperates with the push pins in a cam-follower mechanicalarrangement. Motion of the pushrod 101 causes the pins to slide withinrespective slots 105 to actuate the jaw members. Other ways ofopening/closing the jaws 110 and 120 are contemplated such as any knowncombinations of mechanical or electro-mechanical arrangement of gears,cams, pulleys, springs and sleeves.

The forceps 10 may also include a trigger assembly 70 that advances aknife 190 disposed within the detachable end effector assembly 100. Oncea tissue seal is formed, the user activates the trigger assembly 70 toseparate the tissue along the tissue seal.

Each jaw member 110 and 120 also includes a sealing surface 112 and 122,respectively, disposed on an inner-facing surface thereof. Sealingsurfaces 112 and 122 cooperate to seal tissue held therebetween upon theapplication of energy. Sealing surfaces 112 and 122 are connected togenerator 20 that communicates energy through the tissue heldtherebetween.

As best seen in FIG. 2, forceps 10 also includes an electrosurgicalcable 11 which connects the forceps 10 to generator 20. Cable 11 isinternally divided into cable leads (not shown) which each transmitelectrosurgical energy through their respective feed paths through theforceps 10 to the detachable end effector assembly 100.

As mentioned above, detachable end effector assembly 100 is attached atthe distal end 14 of shaft 12 and includes a pair of opposing jawmembers 110 and 120. As described above, movable handles 62 and 72mechanically cooperate to impart movement of the jaw members 110 and 120from an open position, wherein the jaw members 110 and 120 are disposedin spaced relation relative to one another, to a clamping or closedposition wherein the jaw members 110 and 120 cooperate to grasp tissuetherebetween.

As shown best in FIGS. 3A-3B, 4 and 5, the detachable end effectorassembly 100 is designed as a bilateral assembly, i.e., both jaw members110 and 120 pivot relative to one another about a pivot pin 95 disposedtherethrough. The jaw members 110 and 120 are curved to facilitatemanipulation of tissue and to provide better “line of sight” foraccessing organs and large tissue structures. In other embodiments, thejaw members 110 and 120 may have a straight configuration.

Push rod 101, which ultimately connects to a drive assembly (not shown),is dimensioned to slidingly receive knife drive rod 193, knife 190 andposts 171 a and 171 b of halves 170 a and 170 b of knife guide 170. Pushrod 101, in turn, is received within shaft 12. Upon actuation of thedrive assembly, the push rod 101 reciprocates which, in turn, causes thepins to ride within slots to open and close the jaw members 110 and 120as desired. The jaw members 110 and 120, in turn, pivot about pivot pin95 disposed through respective pivot holes 113 a and 123 a disposedwithin flanges 113 and 123.

Jaw members 110 and 120 are electrically isolated from one another suchthat electrosurgical energy can be effectively transferred through thetissue to form a tissue seal. Jaw members 110 and 120 are engaged to theend of rotating shaft 12 by pivot pin 95 such that rotation of therotating assembly 80 correspondingly rotates shaft 12 (along with pushrod 101 and knife 190) which, in turn, rotates detachable end effectorassembly 100 (See FIG. 2).

FIG. 6 illustrates the in vivo detachable end effector assembly 100 andthe distal end 14 of shaft 12 of the endoscopic surgical instrument orforceps 10 that is generally joined by a coupling 200 according to oneembodiment of the present disclosure. The coupling 200 has an orifice202 a at proximal end 202 and an orifice 212 a at distal end 212. Theorifice 202 a at proximal end 202 is configured to receive the distalend 14 of shaft 12 of the endoscopic surgical instrument or forceps 10while the orifice 212 a at distal end 212 is configured to receiveproximal end 1250 of the shaft 1201 of the detachable end effectorassembly 100. As previously described above with respect to FIGS. 3A and3B, detachable end effector assembly 100 includes proximal end 1250comprising shaft 1201 at proximal end 1250 that is configured to engagedistal end 14 of the shaft 12 of the forceps 10 at interface joint 140.The engagement between the shaft 12 and the shaft 1201 enables theattachment and detachment of the end effector assembly 100 with theforceps 10 during an in vivo surgical procedure. The installation of thecoupling 200 during the in vivo surgical procedure thereby secures thejoint 140 and enables the attachment of the end effector assembly 100 tothe shaft 12 of the forceps 10. Conversely, release of the coupling 200upon completion of activities required using the forceps 10 during thein vivo surgical procedure enables the detachment of the end effectorassembly 100 from the shaft 12 of the forceps 10. To assist in theinstallation of the coupling 200, one or more alignment indicators,e.g., an arrow 1210 formed at an appropriate location on the shaft 1201of the end effector assembly 100 and a corresponding arrow 1210′ formedon the shaft 12 of the forceps 10, facilitate engagement of the endeffector assembly 100 with the forceps 10 during an in vivo surgicalprocedure.

FIG. 7 illustrates the in vivo detachable end effector assembly 100 andthe shaft 12 of forceps 10 joined at interface joint 140 by an examplecoupling, e.g., a compression coupling 200′ that may have a compressionfitting at one or both ends or a compression fitting at one end andanother type of fitting such as a screw threaded fitting at the otherend, according to one embodiment of the present disclosure. Numerousother suitable couplings may be employed to perform the joining of theend effector assembly 100 and the shaft 12, including, but not limitedto, Luer lock fittings, snap-fit coupling, ball and socket fittings andthe like.

The shaft 12 and the end effector assembly 100 are configured such thatengagement of the end effector assembly 100 with the distal end 14 ofthe shaft 12 establishes electrical communication between the forceps 10and the tissue sealing surface 112 and/or 122 of the end effectorassembly 100.

As also described above previously, the distal end 14 of the shaft 12 isconfigured to interface with coupling 200. The coupling 200 isconfigured to interface with the end effector assembly 100. The endeffector assembly 100 is configured to detachably engage and disengagefrom the distal end 14 of the shaft 12 via engagement of the endeffector assembly 100 with the coupling 200.

The shaft 12 and the end effector assembly 100 are configured such thatengagement of the end effector assembly 100 with the distal end 14 ofthe shaft 12 via the coupling 200 establishes electrical communicationbetween the forceps 10 and the end effector assembly 100.

To accomplish the intended purpose of the combination forceps and invivo detachable end effector assembly 5 (see FIG. 2), the end effectorassembly 100 may be configured to vary the ratio between the moment ofinertia of the cross-section of the end effector assembly and the momentof inertia of the cross-section of the shaft 12 depending on anyparticular surgical purpose.

In addition, coupling 200 may be configured to selectively engage afirst end effector assembly having a cross-sectional moment of inertiavalue and a second end effector assembly having a cross-sectional momentof inertia value that differs from the cross-sectional moment of inertiavalue of the first end effector assembly. That is, the coupling may be auniversal type coupling configured to selectively engage end effectorassemblies of different or various sizes.

FIGS. 8-10 illustrate simplified views of portions of the in vivo methodof attaching the detachable end effector assembly 100 to the forceps 10to form the combination forceps and end effector assembly 5 (see FIG. 2)for use during the surgical procedure to seal and cut tissue.

More particularly, FIG. 8 is a simplified view of an abdominal cavity Cin a subject illustrating the in vivo method of attaching detachable endeffector assembly 100 to forceps 10 during a laparoscopic procedureaccording to one embodiment of the present disclosure. A surgical handaccess apparatus 400 is shown installed within an opening or surgicalincision I_(A) in abdominal wall W located at a position such as at thenavel of the subject as shown. Such a surgical hand access apparatus andthe method of installation are described in commonly-owned U.S. PatentApplication Publication US 2006/0229501 A1, by Jensen et al., entitled“SURGICAL HAND ACCESS APPARATUS”, now U.S. Pat. No. 7,766,824 issued onAug. 3, 2010. The hand H of a surgeon is illustrated grasping the invivo detachable end effector assembly 100 and inserting or positioningthe end effector assembly 100 through the incision I_(A) and into theabdominal cavity C. The end effector assembly 100 is grasped andoriented in a position to facilitate attachment and engagement of theend effector assembly 100 with the forceps 10.

The forceps 10 is provided and inserted, minus the detachable endeffector assembly 100, through another opening or incision I_(B) in thebody that allows the surgeon to position the distal end 14 of the shaft12 such that upon attachment and engagement of the end effector assembly100 to the shaft 12, the resulting combination forceps and end effectorassembly 5 (see FIG. 2) is advantageously positioned to perform thedesired surgical procedure.

Although not shown, the method further includes the step of engaging theend effector assembly 100 with the distal end 14 of the shaft 12. Thestep of engaging the end effector assembly 100 with the distal end 14 ofthe shaft 12 enables establishment of electrical communication betweenthe forceps 10 and the tissue sealing surface 112 and/or 122 of jawmembers 110 and/or 120 of the end effector assembly 100.

When at least one jaw member, e.g., lower jaw member 120, of the endeffector assembly 100 further includes a mechanical cutting element,e.g., knife blade 190, the step of engaging the end effector assembly100 with the distal end 14 of the shaft 12 also enables establishment ofmechanical communication between the forceps 10 and the mechanicalcutting element of the jaw member 120 to enable mechanical cutting oftissue.

As described above to assist in the installation of the coupling 200,the method may include providing one or more alignment indicators, e.g.,arrow 1210 formed at an appropriate location on the shaft 1201 of theend effector assembly 100 and/or corresponding arrow 1210′ formed on theshaft 12 of the forceps 10, to facilitate engagement of the end effectorassembly 100 with the forceps 10 during an in vivo surgical procedure.The step of aligning the end effector assembly 100 with the forceps 10may include rotating the end effector assembly 100, in the directionindicated by arrow B around longitudinal axis A of the end effectorassembly 100, and also translating the end effector assembly 100 in thedirection of the longitudinal axis A, as illustrated in FIGS. 6 and 7.

To further assist the surgeon in implementing the attachment andengagement of the end effector assembly 100 to the shaft 12 and inimplementing the surgical procedure, an endoscopic camera 250 may bepositioned and inserted through the abdominal wall W into the abdominalcavity C through another opening or incision I_(C) in the body at anopposite side of the abdominal wall W to facilitate transmission oflight L towards the end effector assembly 100 and the distal end 14 ofthe shaft 12 and to facilitate reception of cinematic images.

FIG. 9 is a simplified view of the abdominal cavity C in a subjectillustrating an in vivo method of attaching, via a grasping device, thedetachable end effector assembly 100 to the forceps 10 during alaparoscopic procedure according to another embodiment of the presentdisclosure. A grasping device 300, such as the endoscopic surgicaldevice having an articulating handle assembly that is disclosed incommonly-owned U.S. patent application Ser. No. 12/193,864 by De Santiset al., filed on Aug. 19, 2008, entitled “ENDOSCOPIC SURGICAL DEVICE”,published on Feb. 26, 2009 as U.S. Patent Application Publication No. US2009/0054734 A1, the entire contents of which are hereby incorporated byreference herein, is positioned and inserted through an opening in thebody such as a natural orifice D, Again, the end effector assembly 100is grasped and oriented in a position to facilitate attachment andengagement of the end effector assembly 100 with the forceps 10.

In a similar manner as described above with respect to FIG. 8, theforceps 10 is provided and inserted, minus the detachable end effectorassembly 100, through opening or incision I_(B) in the body that allowsthe surgeon to position the distal end 14 of the shaft 12 such that uponattachment and engagement of the end effector assembly 100 to the shaft12, the resulting combination forceps and end effector assembly 5 (seeFIG. 2) is advantageously positioned to perform the desired surgicalprocedure.

Again, although not shown, the method may further include the step ofengaging the end effector assembly 100 with the distal end 14 of theshaft 12. The step of engaging the end effector assembly 100 with thedistal end 14 of the shaft 12 enables establishment of electricalcommunication between the forceps 10 and the end effector assembly 100.

In a similar manner, when at least one jaw member, e.g., lower jawmember 120, of the end effector assembly 100 further includes amechanical cutting element, e.g., knife blade 190, the step of engagingthe end effector assembly 100 with the distal end 14 of the shaft 12also enables establishment of mechanical communication between theforceps 10 and the mechanical cutting element (knife blade 190) of thejaw member 120 to enable mechanical cutting of tissue.

FIG. 10 is a simplified view of the adominal cavity C in a subjectillustrating an alternative in viva method of attaching the detachableend effector assembly 100 to forceps 10 during a laparoscopic procedure,as compared to the in vivo method described above with respect to FIG.9, via the coupling 200 that is configured to interface with the endeffector assembly 100 and the forceps 10, according to still anotherembodiment of the present disclosure.

As described previously above with respect to FIGS. 6 and 7, the endeffector assembly 100 and the distal end 14 of the shaft 12 of theforceps 10 are configured to interface with the coupling 200. As can beappreciated, the previous steps of implementing the method of engagingthe forceps 10 with the end effector assembly 100 described above withrespect to FIG. 9 are each implemented by interfacing the coupling 200with the end effector assembly 100 and with the distal end 14 of theshaft 12.

The methods described above with respect to FIGS. 8-10 may beimplemented wherein forceps 10 includes trigger assembly 70 (thatincludes a trigger—see FIG. 2) operably coupled to the housing 60 andthe end effector assembly 100 includes a knife 192 (see FIG. 4) and themethod includes the step of actuating the trigger 70 to advance theknife 192 to separate tissue disposed in the end effector assembly 100.

Additionally, the method may be implemented by providing coupling 200configured to selectively engage a first end effector assembly having across-sectional moment of inertia value and a second end effectorassembly having a cross-sectional moment of inertia value that differsfrom the cross-sectional moment of inertia value of the first endeffector assembly depending on a surgical need. That is, as describedpreviously, the coupling 200 may be a universal type coupling configuredto selectively engage end effector assemblies of different or varioussizes depending on the requirements for a particular surgical procedureor need.

Actuation of the handles 62 and 72 closes the jaw members 110 and 120about tissue with a pre-determinable and consistent closure pressure toeffect a tissue seal. Closure pressures for sealing large tissuestructures fall within the range of about 3 kg/cm² to about 16 kg/cm².

Stop members 90 which extend from the sealing surface 122 provide aconsistent and accurate gap distance “G” (not shown) between theelectrically conductive sealing surfaces 112 and in the range from about0.001 inches (about 0.0254 millimeters) to about 0.006 inches (about0.1524 millimeters) which is also effective for sealing tissue.

After the tissue is grasped between jaw members 110 and 120, the forceps10 is ready for selective application of electrosurgical energy andsubsequent separation of the tissue. By controlling the intensity,frequency and duration of the electrosurgical energy and pressureapplied to the tissue, the user can effectively seal tissue.

Referring to FIG. 2, it can be appreciated from the foregoing that theembodiments of the present disclosure may include a kit for an in vivosurgical procedure that includes forceps 10 having housing 60 includingshaft 12 that extends therefrom and at least one handle 62 that ismovable relative to the housing 60. The kit also includes theselectively engageable end effector assembly 100 that is configured toselectively engage the distal end 14 of the shaft 12. The kit mayfurther include coupling 200 that is configured to facilitate engagementof the end effector assembly 100 to the forceps 10.

The state of the art of endoscopic surgery is advanced by theembodiments of the present disclosure, since the embodiments of thepresent disclosure enable removing the diameter and length constraintsof the end effectors of the prior art to generally allow for loosertolerances and more cost effective end effector fabrication processes.As described above, the diameter is a significant factor in determiningthe necessary rigidity of the end effector assembly, so that alarger-diameter end effector assembly can be a longer end effectorassembly because the end effector assembly will be less susceptible todeflection and thus will provide a more uniform distribution of sealingpressure to the tissue.

While several embodiments of the disclosure have been shown in thedrawings and/or discussed herein, it is not intended that the disclosurebe limited thereto, as it is intended that the disclosure be as broad inscope as the art will allow and that the specification be read likewise.Therefore, the above description should not be construed as limiting,but merely as exemplifications of particular embodiments. Those skilledin the art will envision other modifications within the scope and spiritof the claims appended hereto.

1. A method of performing surgery, comprising the steps of: providing aninstrument having a housing including a shaft that extends therefrom;providing a treatment member configured to selectively engage a distalend of the shaft; inserting the instrument through a first openingformed in a body; inserting the treatment member through a secondopening formed in the body; engaging the instrument with the distal endof the shaft in vivo; and engaging the treatment member to treat tissue.2. A method of performing surgery according to claim 1, wherein the stepof engaging the treatment member with the shaft establishes anelectro-mechanical connection for electrosurgically treating tissue. 3.A method of performing surgery according to claim 1, wherein thetreatment member is adapted to connect to an electrosurgical energysource and the method further includes the step of activating thetreatment member, via the electrosurgical energy source, to treattissue.
 4. A method of performing surgery according to claim 1, whereinthe step of inserting the instrument through a first opening formed in abody is performed by inserting the instrument through a natural bodyorifice.
 5. A method of performing surgery according to claim 1, whereinthe step of inserting the treatment member through a second openingformed in the body is performed by inserting the treatment memberthrough a natural body orifice.
 6. A method of performing surgeryaccording to claim 1, wherein the method includes the step of insertinga camera through a third opening in the body.
 7. A method of performingsurgery according to claim 6, further comprising the step ofvisualizing, via the camera, engagement of the treatment member with thedistal end of the shaft.
 8. A method of performing surgery according toclaim 1, further comprising the step of inserting a grasping devicethrough a third opening in the body.
 9. A method of performing surgeryaccording to claim 8, wherein the step of inserting the grasping devicethrough a third opening in the body is performed by grasping thetreatment member via the grasping device and inserting the treatmentmember through a third opening in the body
 10. A method of performingsurgery according to claim 9, further comprising the step of engagingthe treatment member with the distal end of the shaft.
 11. A method ofperforming surgery according to claim 1, further comprising the step ofproviding a coupling at the distal end of the shaft.
 12. A method ofperforming surgery according to claim 11, further comprising the step ofengaging, via the coupling, the distal end of the shaft with thetreatment member.
 13. A method of performing surgery according to claim11, wherein the step of providing a coupling at the distal end of theshaft is performed by providing at least one of a Luer-lock coupling, athreaded coupling, a compression coupling, a snap-fit coupling, aslide-fit coupling and a magnetic coupling.
 14. A method of performingsurgery according to claim 1, wherein the instrument includes a triggeroperably coupled to the housing and the treatment member includes aknife and the method includes the step of actuating the trigger toadvance the knife to separate tissue disposed in the treatment member.15. A method of performing surgery according to claim 1, furthercomprising the step of providing an alignment indicator to at least oneof the instrument and the treatment member to facilitate engagementbetween the instrument and the treatment member.
 16. A method ofperforming surgery according to claim 15, further comprising the step ofaligning the instrument and the treatment member.
 17. A method ofperforming surgery according to claim 16, further comprising the step ofengaging the instrument and the treatment member.
 18. A method ofperforming surgery according to claim 11, wherein the step of providinga coupling at the distal end of the shaft is performed by providing acoupling configured to selectively engage a first treatment memberhaving a cross-sectional moment of inertia and a second treatment memberhaving a cross-sectional moment of inertia that differs from thecross-sectional moment of inertia of the first treatment member.